MODIFIED SERIES 2100 ENDOSCOPES— 510(k) K912089

Substantially Equivalent

Medical Laser, Inc.

FDA 510(k) clearance K912089 for MODIFIED SERIES 2100 ENDOSCOPES, Substantially Equivalent on 1991-08-12. Applicant: Medical Laser, Inc..

Clearance details

Applicant: Medical Laser, Inc.
Product code: Code ODF
Advisory panel: Gastroenterology, Urology
Date received: 1991-05-13
Decision date: 1991-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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